147 related articles for article (PubMed ID: 15368487)
21. Mutation detection of GJB2 using IsoCode and real-time quantitative polymerase chain reaction with SYBR green I dye for newborn hearing screening.
Kudo T; Oshima T; Kure S; Matsubara Y; Ikeda K
Laryngoscope; 2004 Jul; 114(7):1299-304. PubMed ID: 15235365
[TBL] [Abstract][Full Text] [Related]
22. Molecular diagnosis of genetic deafness.
Jonard L; Marlin S; Louha M; Bonnet C; Couderc R; Garabedian N; Denoyelle F;
Clin Biochem; 2011 May; 44(7):510-511. PubMed ID: 22036352
[No Abstract] [Full Text] [Related]
23. Diagnostic application of targeted resequencing for familial nonsyndromic hearing loss.
Choi BY; Park G; Gim J; Kim AR; Kim BJ; Kim HS; Park JH; Park T; Oh SH; Han KH; Park WY
PLoS One; 2013; 8(8):e68692. PubMed ID: 23990876
[TBL] [Abstract][Full Text] [Related]
24. Large scale newborn deafness genetic screening of 142,417 neonates in Wuhan, China.
Hao Z; Fu D; Ming Y; Yang J; Huang Q; Lin W; Zhang H; Zhang B; Zhou A; Hu X; Yao C; Dong Y; Ring HZ; Ring BZ
PLoS One; 2018; 13(4):e0195740. PubMed ID: 29634755
[TBL] [Abstract][Full Text] [Related]
25. Genetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA).
Prasad S; Cucci RA; Green GE; Smith RJ
Hum Mutat; 2000 Dec; 16(6):502-8. PubMed ID: 11102979
[TBL] [Abstract][Full Text] [Related]
26. Molecular diagnosis of deafness: impact of gene identification.
Usami S; Koda E; Tsukamoto K; Otsuka A; Yuge I; Asamura K; Abe S; Akita J; Namba A
Audiol Neurootol; 2002; 7(3):185-90. PubMed ID: 12053143
[TBL] [Abstract][Full Text] [Related]
27. Genetic screening involving 101 hot spots for neonates not passing newborn hearing screening and those random recruited in Dongguan.
Liu Y; Ye L; Zhu P; Wu J; Tan S; Chen J; Wu C; Zhong Y; Wang Y; Li X; Liu H
Int J Pediatr Otorhinolaryngol; 2019 Feb; 117():82-87. PubMed ID: 30579095
[TBL] [Abstract][Full Text] [Related]
28. [Analysis of deafness gene mutations by gene chip and its clinical significance].
Zhang H; Liu Y; Wang Y; Li G; Luo Z; Jiang Pf; Li F; Wang S; Deng K
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2009 Nov; 23(22):1032-5. PubMed ID: 20359100
[TBL] [Abstract][Full Text] [Related]
29. [Analysis of deafness-related gene mutations in 100 non-syndromic hearing loss patients in Henan province].
Yang A; Geng M; Zhang H; Guo X; Tang J; Han F
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Nov; 29(22):1959-62. PubMed ID: 26911058
[TBL] [Abstract][Full Text] [Related]
30. Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.
Green GE; Scott DA; McDonald JM; Woodworth GG; Sheffield VC; Smith RJ
JAMA; 1999 Jun; 281(23):2211-6. PubMed ID: 10376574
[TBL] [Abstract][Full Text] [Related]
31. Common molecular etiology of patients with nonsyndromic hearing loss in Tibetan, Tu nationality, and Mongolian patients in the northwest of China.
Yang XL; Bai-Cheng X; Chen XJ; Pan-Pan B; Jian-Li M; Xiao-Wen L; Zhang ZW; Wan D; Zhu YM; Guo YF
Acta Otolaryngol; 2013 Sep; 133(9):930-4. PubMed ID: 23834103
[TBL] [Abstract][Full Text] [Related]
32. Ethnic-specific spectrum of GJB2 and SLC26A4 mutations: their origin and a literature review.
Tsukada K; Nishio SY; Hattori M; Usami S
Ann Otol Rhinol Laryngol; 2015 May; 124 Suppl 1():61S-76S. PubMed ID: 25999548
[TBL] [Abstract][Full Text] [Related]
33. [Analysis and prenatal diagnosis of deafness-related gene mutations in patients with nonsyndromic hearing loss].
Li H; Chen Y; Mao Y; Ding Y; Xu X; Tang S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):553-6. PubMed ID: 25297579
[TBL] [Abstract][Full Text] [Related]
34. [Genetic diagnosis of deafness].
Usami S
Nihon Rinsho; 2005 Dec; 63 Suppl 12():258-63. PubMed ID: 16416804
[No Abstract] [Full Text] [Related]
35. [Current status of newborn deafness gene screeningin parts of China].
Wen C; Huang L; Xie S; Zhao X; Yu Y; Cheng X; Guo L; Nie W; Ge F; Wang C; Liu Q; Hu S; Chen Y; Gao M; Han J
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2020 Nov; 34(11):972-977. PubMed ID: 33254312
[No Abstract] [Full Text] [Related]
36. [Analysis of deafness-related gene mutations in 23 nonsyndromic hearing impairment families in Guangxi Zhuang Autonomous Region].
Shi M; Liu F; Xu L; Liu M; Tang FZ; Liang JP; Lu QT; Zhai SH; Huang J; Chen RC
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2017 Feb; 31(4):277-283. PubMed ID: 29871242
[No Abstract] [Full Text] [Related]
37. SNPscan as a high-performance screening tool for mutation hotspots of hearing loss-associated genes.
Li H; Wang B; Liu D; Wang T; Li Q; Wang W; Li H
Genomics; 2015 Aug; 106(2):83-7. PubMed ID: 26004784
[TBL] [Abstract][Full Text] [Related]
38. Rapid umbilical cord diagnostic of hereditary profound hearing loss: how we do it.
Birkenhäger R; Maier W; Kunze M; Aschendorff A; Arndt S
Clin Otolaryngol; 2009 Aug; 34(4):374-6. PubMed ID: 19673989
[No Abstract] [Full Text] [Related]
39. Analysis of common deafness gene mutations in deaf people from unique ethnic groups in Gansu Province, China.
Xu BC; Bian PP; Liu XW; Zhu YM; Yang XL; Ma JL; Chen XJ; Wang YL; Guo YF
Acta Otolaryngol; 2014 Sep; 134(9):924-9. PubMed ID: 24941117
[TBL] [Abstract][Full Text] [Related]
40. Molecular genetic landscape of hereditary hearing loss in Pakistan.
Naz S
Hum Genet; 2022 Apr; 141(3-4):633-648. PubMed ID: 34308486
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
